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Assistant Icon Designer Jobs (NOW HIRING)

ICON

Study Lead Biostatistician

Blue Bell, PA · On-site +1

Be familiar with statistical policy and strategy at Amgen * Assist with study and systems audits ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

ICON

Senior Contract Analyst

Blue Bell, PA · On-site +1

$84K - $111K/yr

... deadlines. * Assist in the development and implementation of contract management processes ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

ICON

CLINICAL TRIAL ASSISTANCE - BASE

Blue Bell, PA · On-site +1

$32 - $43.75/hr

Key responsibilities include: * Assist in the planning, execution, and monitoring of clinical ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

ICON

Clinical Research Associate

Miami, FL · On-site +1

Document site progress and escalate risks or issues to the clinical team * Assist in tracking site ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

ICON

Senior Clinical Research Associate

Knoxville, TN · On-site +1

Document site progress and escalate risks or issues to the clinical team * Assist in tracking site ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

ICON

Clinical Research Associate II

Chicago, IL · On-site +1

$91K - $114K/yr

Document site progress and escalate risks or issues to the clinical team * Assist in tracking site ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

ICON

Clinical Research Associate

Detroit, MI · On-site +1

Document site progress and escalate risks or issues to the clinical team * Assist in tracking site ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

ICON

Senior Clinical Research Associate

Los Angeles, CA · On-site +1

$110K - $138K/yr

Document site progress and escalate risks or issues to the clinical team * Assist in tracking site ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

ICON

Clinical Research Associate II

Los Angeles, CA · On-site +1

$91K - $114K/yr

Document site progress and escalate risks or issues to the clinical team * Assist in tracking site ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

ICON

Scientist III

New York, NY · On-site

$68K - $85K/yr

Interact with clients to transmit study status and results. • *Assist in the definition and ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

ICON

Clinical Research Associate II

West Palm Beach, FL · On-site +1

Document site progress and escalate risks or issues to the clinical team * Assist in tracking site ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

ICON

Senior Clinical Research Associate

Los Angeles, CA · On-site +1

$110K - $138K/yr

Document site progress and escalate risks or issues to the clinical team * Assist in tracking site ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

Icon plc

Production Associate

Farmingdale, NY · On-site

$21.50/hr

What You Will Do: * Assist in the coordination of production activities, including tracking ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

ICON

Senior Medical Research Associate

Lenexa, KS · On-site

Research & Operational Responsibilities * Assist in planning, coordinating, and executing clinical ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

ICON

Facilities & Admin Coordinator

Lenexa, KS · On-site

Keep management informed of any issues within the organization that require attention * Assist with ... salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive ...

ICON

Lab Analyst II

Lenexa, KS · On-site

... compendial methods. * Assist in developing pharmaceutical formulations by testing various ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

ICON

Senior Clinical Trial Manager

Blue Bell, PA · On-site +1

... assist with documentation, such as storyboards, lessons-learned, metrics, etc., that may be ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

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As of Jun 20, 2026, the average hourly pay for assistant icon designer in the United States is $24.63, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $28.61 per hour, depending on experience, location, and employer.
What are the most commonly searched types of Icon Designer jobs? The most popular types of Icon Designer jobs are:
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Infographic showing various Assistant Icon Designer job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, and 99% Full Time. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $51,223 per year, or $24.6 per hour.
Study Lead Biostatistician

Study Lead Biostatistician

ICON

Blue Bell, PA • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 23 days ago

Job description

Study Lead Biostatistician
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Principal Biostatistician at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. This position is sitting within the Biosimilars group.
What You Will Do:
  • Strong ability to apply statistics in the analysis of clinical trials
  • Independent leadership of the design, analysis and reporting of at least 1 complex or multiple less complex studies/projects within the Pharmaceutical/Biotechnology/Public Health setting in Industry, Government or Academia
  • Demonstrated ability to provide sound strategic and statistical input on study/research design to meet project needs, regulatory and scientific requirements
  • Demonstrated ability in presenting results and defending statistical findings, study design and analysis. This could be to internal audiences (study/product team) OR at external meetings such as investigator meetings, steering committee meetings, ad board meetings or regulatory meetings
  • Excellent oral and written English communication skills
  • Authored a protocol, DRT/DMC charter, SAP, CSR, or Research Project Plan (RPP)
  • Strong knowledge of current CDISC standards for ADaMs
  • Strong fundamentals of Project Planning and Project Management
  • Demonstrated ability to immediately dive into detailed and/or complex projects
  • Strong SAS programming skills in applying statistical procedures based on complex study designs
  • Perform all duties and responsibilities associated with the Study Supporting Statistician role
  • Oversee the work performed by multiple Study Supporting Statisticians
  • Review work performed by Study Supporting Statistician and provide guidance to meet the study and project requirements
  • Attend Clinical Study Team (CST) meetings and provide all required statistical input related to strategy and operations of the clinical study
  • Plan and execute statistical contributions to Study Outlines, protocols, randomization specifications, Statistical Analysis Plans (SAPs), Table, Listing and Graph ( TLG) shells, Submission Data File (SDF) specifications, other key- study related documentation, protocol deviations, Data Quality Review (DQR), Flash Memos, Clinical Study Reports (CSRs), clinical publications, product plans (e.g. Global Development Plan), Clinical Summary of Safety (CSSs), Clinical Summary of Efficacy (CSEs), Clinical Overviews (COs), regulatory documents, reimbursement documents and other communications
  • Assist in resource planning for assigned projects
  • Be familiar with all Company's policies, SOPs and other controlled documents related to all study activities performed
  • Be familiar with statistical policy and strategy at Amgen
  • Assist with study and systems audits conducted by Company GCA and external bodies
  • Stay abreast of latest developments in the field of statistics in drug development

Your Profile:
  • Master's degree in Statistics/Biostatistics or other subject with high statistical content with 6 years of post-graduate statistical experience in the pharmaceutical industry or medical research OR Doctoral degree in Statistics/Biostatistics or other subject with high statistical content with 3 years of post-graduate statistical experience in the pharmaceutical industry or medical research
  • Strong skill in communicating statistical information clearly and concisely (written and oral)
  • Strong understanding of statistical concepts related to the design and conduct of clinical studies

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply

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